Kartagener’s Syndrome: A Case Report
Abstract
Kartagener’s Syndrome is a subgroup of primary ciliary dyskinesias (PCD) which is characterised by impairment of mucociliary clearance. It is a rare, autosomal recessive disorder characterised by triad of situs invertus, chronic sinusitis and bronchiectasis. We report a case of this rare entity. Need for early diagnosis, appropriate respiratory management and timely treatment of infertility in these patients constitutes comprehensive management.
References
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2. Corkey CW, Levison H, Turner JA. The immotile cilia syndrome. A longitudinal survey. Am Rev Respir Dis. 1981; 124:544.
3. Barthwal MS. Kartagener’s syndrome in a fertile male - An uncommon variant. Lung India. 2006;23:123-5.
4. Amit A. Palange, Mohd. Shahid, Manjit S. Sisode, BhumikaVaishnav. Kartagener’s syndrome: Case Report. Int’l J. of Healthcare & Biomedical Research. 2013;2: 67-69.
5. Marthin JK, Petersen N, Skovgaard LT, Nielsen KG. Lung function in patients with primary ciliary dyskinesia: A crosssectional and 3-decade longitudinal study. Am J RespirCrit Care Med. 2010;181:1262–8.
6. Barbato A, Frischer T, Kuehni CE, Snijders D, Azevedo I, Baktai G, et al. Primary ciliary dyskinesia: A consensus statement on diagnostic and treatment approaches in children. Eur Respir J. 2009;34:1264-76.
Published
2019-08-27
How to Cite
Tyagi R, Sahu S. (2019). Kartagener’s Syndrome: A Case Report. The Indian Practitioner, 68(4), 38-39. Retrieved from https://articles.theindianpractitioner.com/index.php/tip/article/view/647
Section
Case Reports
